SCOPUS 정보 검색 플랫폼

Journal of Human Genetics

Volumn 43, Issue 4, 1998, Pages 224-227

New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardation

(2) Tsukahara, Masato a Sugio, Yoshitsugu b

a YAMAGUCHI UNIVERSITY (Japan)

b Ogori Daiichi General Hospital (Japan)

Author keywords

Dominant inheritance; Facial abnormality; Mental retardation; Microcephaly; Micromelia

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHILD; COMPUTER ASSISTED TOMOGRAPHY; DERMATOGLYPHICS; DOMINANT INHERITANCE; FACE MALFORMATION; FEMALE; HUMAN; INTELLIGENCE QUOTIENT; MALE; MENTAL DEFICIENCY; MICROCEPHALY; MICROMELIA; PEDIGREE; RADIOGRAPHY; SYNDROME;

ADULT; CHILD; CHILD, PRESCHOOL; FACE; FEMALE; GENES, DOMINANT; HUMANS; LIMB DEFORMITIES, CONGENITAL; MALE; MENTAL RETARDATION; MICROCEPHALY; PEDIGREE; SYNDROME;

COLUMELLA;

EID: 0031675398 PISSN: 14345161 EISSN: None Source Type: Journal
DOI: 10.1007/s100380050077 Document Type: Article

Times cited : (2)

References (4)

1
- 0027423908
- Brachmann-de Lange syndrome Delineation of the clinical phenotype
- Ireland M, Donnai D, Burn J (1993) Brachmann-de Lange syndrome Delineation of the clinical phenotype. Am J Med Genet 47: 959-964
- (1993) Am J Med Genet , vol.47 , pp. 959-964
- Ireland, M.¹ Donnai, D.² Burn, J.³

2
- 0023214677
- Syndrome of microcephaly, deafness/ malformed ears, mental retardation and peculiar facies in a mother and son
- Kawashima H, Tsuji N (1987) Syndrome of microcephaly, deafness/ malformed ears, mental retardation and peculiar facies in a mother and son. Clin Genet 31: 303-307
- (1987) Clin Genet , vol.31 , pp. 303-307
- Kawashima, H.¹ Tsuji, N.²

3
- 0001960990
- The C syndrome of multiple congenital anomalies
- Opitz JM, Johnson RC, McCreadie SR, Smith DW (1969) The C syndrome of multiple congenital anomalies. Birth Defects Orig Art Ser V(2) 161-166
- (1969) Birth Defects Orig Art Ser , vol.5 , Issue.2 , pp. 161-166
- Opitz, J.M.¹ Johnson, R.C.² McCreadie, S.R.³ Smith, D.W.⁴

4
- 0027366126
- Clinical variability within Brachmann-de Lange syndrome: A proposed classification system
- Van Allen MI, Filippi G, Siegel-Bartelt J, Yong S-L, McGillivray B, Zuker RM, Smith CR, Magee JF, Ritchie S, Toi A, Reynolds JF (1993) Clinical variability within Brachmann-de Lange syndrome: A proposed classification system. Am J Med Genet 47: 947-958
- (1993) Am J Med Genet , vol.47 , pp. 947-958
- Van Allen, M.I.¹ Filippi, G.² Siegel-Bartelt, J.³ Yong, S.-L.⁴ McGillivray, B.⁵ Zuker, R.M.⁶ Smith, C.R.⁷ Magee, J.F.⁸ Ritchie, S.⁹ Toi, A.¹⁰ Reynolds, J.F.¹¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.